The following data is part of a premarket notification filed by Fresenius Usa, Inc. with the FDA for Fresenius Hemoflow, F40m, F50m, F60m & F80m.
| Device ID | K892262 |
| 510k Number | K892262 |
| Device Name: | FRESENIUS HEMOFLOW, F40M, F50M, F60M & F80M |
| Classification | Dialyzer, High Permeability With Or Without Sealed Dialysate System |
| Applicant | FRESENIUS USA, INC. 4090 PIKE LN. Concord, CA 94520 |
| Contact | Scott N Walker |
| Correspondent | Scott N Walker FRESENIUS USA, INC. 4090 PIKE LN. Concord, CA 94520 |
| Product Code | KDI |
| CFR Regulation Number | 876.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-04-05 |
| Decision Date | 1989-04-25 |